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    • 1. 发明申请
    • NOVEL ERGOLINE DERIVATIVES AND USES THEREOF
    • 新颖的胆固醇衍生物及其用途
    • US20140179707A1
    • 2014-06-26
    • US14134127
    • 2013-12-19
    • MAP PHARMACEUTICALS, INC.
    • Thomas ArmerShashidhar KoriLibo Wu
    • A61K31/4985A61M15/00
    • A61K31/4985
    • Provided herein are 8′-Hydroxy-2-CF3-dihydroergotamine (8′OH-2-CF3-DHE) compounds, compositions, and dosage forms containing such compositions. Also provided herein are methods of treatment, prevention, or amelioration of a variety of medical disorders such as, for example, migraine using the compounds and compositions disclosed herein. In still other embodiments, provided herein are methods of agonizing receptors such as, for example, the 5-HT1D and/or the 5-HT1B receptor, without agonizing the 5-HT2B receptor using the compounds and compositions disclosed herein. In still other embodiments, provided herein are methods of antagonizing or inhibiting activity at receptors such as, for example, the adrenergic alpha2A and/or the alpha2B receptors using the compounds and compositions disclosed herein.
    • 本文提供了含有这种组合物的8'-羟基-2- CF 3 - 二氢麦角胺(8'OH-2-CF3-DHE)化合物,组合物和剂型。 本文还提供了使用本文公开的化合物和组合物治疗,预防或改善各种医学病症例如偏头痛的方法。 在其它实施方案中,本文提供的是使用本文公开的化合物和组合物来激发受体例如5-HT1D和/或5-HT1B受体而不激发5-HT 2B受体的方法。 在其它实施方案中,本文提供了使用本文公开的化合物和组合物来拮抗或抑制受体例如肾上腺素α2A和/或α2B受体的活性的方法。
    • 2. 发明申请
    • NOVEL ERGOLINE DERIVATIVES AND USES THEREOF
    • 新颖的胆固醇衍生物及其用途
    • US20150238487A1
    • 2015-08-27
    • US14697906
    • 2015-04-28
    • MAP Pharmaceuticals, Inc.
    • Thomas ArmerShashidhar KoriLibo Wu
    • A61K31/4985
    • A61K31/4985
    • Provided herein are 8′-Hydroxy-2-CF3-dihydroergotamine (8′OH-2-CF3-DHE) compounds, compositions, and dosage forms containing such compositions. Also provided herein are methods of treatment, prevention, or amelioration of a variety of medical disorders such as, for example, migraine using the compounds and compositions disclosed herein. In still other embodiments, provided herein are methods of agonizing receptors such as, for example, the 5-HT1D and/or the 5-HT1B receptor, without agonizing the 5-HT2B receptor using the compounds and compositions disclosed herein. In still other embodiments, provided herein are methods of antagonizing or inhibiting activity at receptors such as, for example, the adrenergic alpha2A and/or the alpha2B receptors using the compounds and compositions disclosed herein.
    • 本文提供了含有这种组合物的8'-羟基-2- CF 3 - 二氢麦角胺(8'OH-2-CF3-DHE)化合物,组合物和剂型。 本文还提供了使用本文公开的化合物和组合物治疗,预防或改善各种医学病症例如偏头痛的方法。 在其它实施方案中,本文提供的是使用本文公开的化合物和组合物来激发受体例如5-HT1D和/或5-HT1B受体而不激发5-HT 2B受体的方法。 在其它实施方案中,本文提供了使用本文公开的化合物和组合物来拮抗或抑制受体例如肾上腺素α2A和/或α2B受体的活性的方法。